CA2541404C - Process and apparatus for cooling and atomizing liquid or pasty-like substances - Google Patents
Process and apparatus for cooling and atomizing liquid or pasty-like substances Download PDFInfo
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- CA2541404C CA2541404C CA2541404A CA2541404A CA2541404C CA 2541404 C CA2541404 C CA 2541404C CA 2541404 A CA2541404 A CA 2541404A CA 2541404 A CA2541404 A CA 2541404A CA 2541404 C CA2541404 C CA 2541404C
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
- B01J2/02—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops
- B01J2/04—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops in a gaseous medium
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25C—PRODUCING, WORKING OR HANDLING ICE
- F25C1/00—Producing ice
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25D—REFRIGERATORS; COLD ROOMS; ICE-BOXES; COOLING OR FREEZING APPARATUS NOT OTHERWISE PROVIDED FOR
- F25D3/00—Devices using other cold materials; Devices using cold-storage bodies
- F25D3/10—Devices using other cold materials; Devices using cold-storage bodies using liquefied gases, e.g. liquid air
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Abstract
A process and an apparatus for the rapid cooling and atomization of liquid or pasty substances, in particular even relatively small amounts of liquid or pasty substances being able to be cooled and atomized economically. Both process and apparatus are particularly useful in the pharmaceutical industry for preparing injectable microparticles of polymer or lipid matrices suitable for the incorporation of active ingredients.
Description
Process and apparatus for cooling and atomizing liquid or pasty-like substances Field of the invention s The invention relates to a process and an apparatus for cooling and atomizing liquid or pasty substances.
Background of the invention Cooling processes are used to modify certain properties of substances. The substances io to be cooled are generally treated in apparatuses whose cooling action is based on heat-transfer processes between coolant and the substance to be cooled at cooling surfaces. The heat or cold transport between coolant and the substance to be cooled is therefore only indirect. A relatively rapid cooling of the substances, which is very frequently required, cannot be achieved by this means. These cooling processes are is also frequently unsuitable for carrying out crystallization or freezing, since insulating deposits form on the cooling surfaces which can impair the cooling process.
Cooling processes of this type are, for example, described in Rompp Chemielexileon (Chemistry lexicon) and Pahlmann, Taschenbuch der Kaltetechnik (Refrigeration manual).
zo It is further lcnown that on an industrial level, spraying (nebulizing) towers are used to produce fme powders with the use of conventional refrigeration.
Cryogenic cooling and freezing processes in which low-temperature gases are used are also prior art. Rompp Chemielexilcon and Pahlmann, Taschenbuch der I~altetechnik, for example, disclose processes in which the substances to be cooled are zs sprayed with the refrigerant, in particular with liquid nitrogen or with solid carbon dioxide in the form of dry ice or snow. The direct contact of the refrigerant with the substances leads to a substantially more rapid cooling of the substances than with the above-mentioned conventional processes. For a relatively rapid cooling of liquid or pasty substances this process also is unsuitable, since the cooling in the interior of the so substances is determined by the heat transport through the substance itself, and the contact surfaces for a rapid cooling, for example for crystallization, are still too small.
It is virtually impossible with these processes to produce readily meterable flowable substances.
The Cryopel° process, described in US 4,967,571, the Cryobrealc°
process, described s in DE 44 19 O10 C1 and the Cryofals° process, described in DE 43 29 110 C1 are known processes in which liquid substances are cooled very rapidly by being introduced drop wise into liquid nitrogen. This cooling process can lead to a meterable pelleted substance. The particle sizes, which are established, are generally in the range of a few millimeters. The cooling is always performed to the temperature io of approximately 77 K, which is not necessary or even undesiderable in a multiplicity of applications.
In addition, an apparatus is known in which a liquid substance is brought into contact with liquid nitrogen, with the use of two jet nozzles, in order to cool the substance rapidly. There is the disadvantage here that the product can be cooled as early as in is the nozzle by the low-temperature nitrogen and can block this nozzle.
A further known process is the Variosol° process, described in EP 1 027 144 B 1, in which the molten substances are mixed with liquid or supercritical carbon dioxide and then expanded in a spray-tower. This expansion causes the cooling and the atomization of the liquid substances, generating fine powders. The use of this process zo for producing microparticles suitable for pharmaceutical purposes, like for example those described in WO 02/051386 has the disadvantage of the non-reproducibility of the particle sizes and the large dimensions of the same.
Description of the invention The object of the invention is to provide a process and an apparatus by which the zs disadvantages of the prior art are overcome and by which a relatively rapid cooling and atomization of liquid or pasty substances is possible, in particular even relatively small amounts of liquid or pasty substances being able to be cooled and atomized economically.
Background of the invention Cooling processes are used to modify certain properties of substances. The substances io to be cooled are generally treated in apparatuses whose cooling action is based on heat-transfer processes between coolant and the substance to be cooled at cooling surfaces. The heat or cold transport between coolant and the substance to be cooled is therefore only indirect. A relatively rapid cooling of the substances, which is very frequently required, cannot be achieved by this means. These cooling processes are is also frequently unsuitable for carrying out crystallization or freezing, since insulating deposits form on the cooling surfaces which can impair the cooling process.
Cooling processes of this type are, for example, described in Rompp Chemielexileon (Chemistry lexicon) and Pahlmann, Taschenbuch der Kaltetechnik (Refrigeration manual).
zo It is further lcnown that on an industrial level, spraying (nebulizing) towers are used to produce fme powders with the use of conventional refrigeration.
Cryogenic cooling and freezing processes in which low-temperature gases are used are also prior art. Rompp Chemielexilcon and Pahlmann, Taschenbuch der I~altetechnik, for example, disclose processes in which the substances to be cooled are zs sprayed with the refrigerant, in particular with liquid nitrogen or with solid carbon dioxide in the form of dry ice or snow. The direct contact of the refrigerant with the substances leads to a substantially more rapid cooling of the substances than with the above-mentioned conventional processes. For a relatively rapid cooling of liquid or pasty substances this process also is unsuitable, since the cooling in the interior of the so substances is determined by the heat transport through the substance itself, and the contact surfaces for a rapid cooling, for example for crystallization, are still too small.
It is virtually impossible with these processes to produce readily meterable flowable substances.
The Cryopel° process, described in US 4,967,571, the Cryobrealc°
process, described s in DE 44 19 O10 C1 and the Cryofals° process, described in DE 43 29 110 C1 are known processes in which liquid substances are cooled very rapidly by being introduced drop wise into liquid nitrogen. This cooling process can lead to a meterable pelleted substance. The particle sizes, which are established, are generally in the range of a few millimeters. The cooling is always performed to the temperature io of approximately 77 K, which is not necessary or even undesiderable in a multiplicity of applications.
In addition, an apparatus is known in which a liquid substance is brought into contact with liquid nitrogen, with the use of two jet nozzles, in order to cool the substance rapidly. There is the disadvantage here that the product can be cooled as early as in is the nozzle by the low-temperature nitrogen and can block this nozzle.
A further known process is the Variosol° process, described in EP 1 027 144 B 1, in which the molten substances are mixed with liquid or supercritical carbon dioxide and then expanded in a spray-tower. This expansion causes the cooling and the atomization of the liquid substances, generating fine powders. The use of this process zo for producing microparticles suitable for pharmaceutical purposes, like for example those described in WO 02/051386 has the disadvantage of the non-reproducibility of the particle sizes and the large dimensions of the same.
Description of the invention The object of the invention is to provide a process and an apparatus by which the zs disadvantages of the prior art are overcome and by which a relatively rapid cooling and atomization of liquid or pasty substances is possible, in particular even relatively small amounts of liquid or pasty substances being able to be cooled and atomized economically.
The object is achieved by a process, in which the liquid or pasty substance/
mixture of substances and gaseous carbon pass, under pressure, through a nozzle and expand in a spray tower. Simultaneously, from a fiu~ther nozzle, liquid carbon dioxide is sprayed in the spray tower. The contact between sprayed liquid or pasty substances/
mixture of s substances and liquid carbon dioxide causes the instantaneous cooling and atomization of the liquid or pasty substances/ mixture of substances. A
schematic representation of the process and apparatus is reported in Figure 1.
During the expansion, small particles of liquid or pasty substances/ mixture of substances, spherically-shaped are formed. This leads to a good reproducibility of the io process and to a fme particulate with an average diameter comprises between 2 and 100 ~.m, preferably in ranges of from 5 to 15 ~.m or from 40 to 80 ~.m, depending on the nozzle used. Moreover, the particles are always spherically shaped and have a narrow particle size distribution.
Therefore the main object of the invention is to provide a process for cooling and is atomizing liquid or pasty substance or mixture of substances, in which a liquid or pasty substance / mixture of substances is combined with gaseous carbon dioxide and the mixture of liquid or pasty substance / mixture of substances and gaseous carbon dioxide is then expanded and cooled by contacting a flux of liquid carbon dioxide, as a result the substance / mixture of substances is cooled and atomized.
zo A further advantage according to the invention is that by varying the flow ratios of substances/ mixture of substances from the first nozzle and the liquid carbon dioxide from the other nozzle, the final temperature obtained may be varied within broad ranges.
It is envisaged that the liquid carbon dioxide has a pressure from 6 to 72 bar and a zs temperature from 216 to 304 K, preferably a pressure from 30 to 70 bar and a temperature from 230 to 304 K, and particularly a pressure from 50 to 68 bar and a temperature from 291 to 301 K.
The pressure of gaseous carbon dioxide in the storage vessel is comprised between 1 to 10 bar, preferably in a range from 1.2 and 4.5 bar. The temperature of the gaseous carbon dioxide in the storage vessel is normally comprised between 273 and 304 K, preferably between 291 and 301 K.
This procedure has the advantage that at a preferred pressure range and temperature range the carbon dioxide can be taken off directly from the supply system, for s example low-pressure and medium-pressure tanks or carbon dioxide cylinders, without further gas treatment.
According to the invention the mixture of liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide and the liquid carbon dioxide are expanded at pressure from 0 to 60 bar, preferably to a pressure from 0 to 20 bar, and particularly to preferably to approximately 1 bar. The expansion to atmospheric pressure (approximately 1 bar) has the advantage that filling can be performed directly into an non-pressurized system.
According to the invention the liquid or pasty substance/ mixture of substances and/or the gaseous carbon dioxide and/or the mixture of liquid or pasty substance/
mixture of is substances and the gaseous carbon dioxide can be fed to al least one heatable or coolable line. Using a heatable or coolable line, the temperature for the liquid or pasty substance/ mixture of substances and/or the gaseous carbon dioxide and/or the mixture of liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide can be controlled, in order to set the desired or required process temperature.
zo According to the invention the liquid or pasty substance/ mixture of substances is mixed with the gaseous carbon dioxide in the storage vessel, thanks to a stirrer disposed in such vessel.
The object is further achieved by an apparatus for cooling liquid or pasty substance or mixture of substances which comprises:
zs a. a storage vessel for the liquid or pasty substance/ mixture of substances, to which is allocated a line, in which a device for transporting the liquid or pasty substance/ mixture of substances is disposed, b. a source of liquid carbon dioxide, to which source is allocated a line, c. a source of gaseous carbon dioxide, to which source is allocated a line which line has a connection with the line transporting the liquid or pasty substance/ mixture of substances, s d. an expansion chamber in which the liquid carbon dioxide and the liquid or pasty substance/ mixture of substances mixed with the gaseous carbon dioxide are conveyed.
The apparatus is constructed in such a manner that the mixture of liquid or pasty substance/ mixture of substances and gaseous carbon dioxide is not expanded until on io exit from the expansion apparatus. A very direct contact takes place out between liquid or pasty substance/ mixture of substances and liquid carbon dioxide achieving cooling and atomization of liquid or pasty substance/ mixture of substances in the spray tower. The apparatus ensures rapid cooling and atomization of the liquid or pasty substance/ mixture of substances. By use of the inventive expansion apparatus, is small, easily flowable particles of the liquid or pasty substance/ mixture of substances are produced.
Advantageously, the lines or apparatuses or devices bearing the liquid or pasty substance/ mixture of substances and/or gaseous carbon dioxide and/or liquid carbon dioxide and/or the lines or apparatuses or devices bearing the mixture of the liquid or ao pasty substance/ mixture of substances and gaseous carbon dioxide have apparatuses for their heating or cooling, in order to set the desired or required temperature in the individual trains bearing carbon dioxide and/or substance/ mixture of substances. The lines) should preferably be heated or cooled separately. Piping having internals for heating is preferred.
zs It is envisaged that an apparatus for heating or cooling is allocated to the line allocated to the storage vessel for the liquid or pasty substance/ mixture of substances.
According to the invention, the expansion apparatus has two valves and two nozzles.
The valves used can be open/closed valve or control valves and they are disposed in the lines connecting the spray tower to the storage vessel and the source of liquid carbon dioxide.
The nozzles for the liquid carbon dioxide and for the mixture of liquid or pasty s substance/ mixture of substances and gaseous carbon dioxide, advantageously, have a shielding device, preferably a jacket tube. The use of a nozzle having a jacket tube has the advantage that only a small amount of air is taken in or sucked into the stream.
The carbon dioxide in this case is at least partially converted into carbon dioxide snow. Typically, approximately 30% by weight of carbon dioxide snow and io approximately 70% by weight of gaseous carbon dioxide are formed during the expansion of the liquid carbon dioxide at the nozzle.
Preferably, the tubes of these expansion devices are prepared. This can be performed by polishing or coating or separate heating. According to the invention a coating with Teflon of the inside of the tubes of the expansion devices are particularly preferred.
is Furthermore, according to the invention, the nozzle for the expansion of the mixture of the liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide, advantageously, has, at its bottom, an isolating coating in order to prevent the obstruction due to the cooled substance on its surface.
According to the invention the nozzle for the expansion of the mixture of the liquid or zo pasty substance/ mixture of substances and the gaseous carbon dioxide can be a capillary flow nozzle or a spraying (nebulizing) nozzle.
The capillary flow nozzle is a one-component nozzle, which diameter is comprised between 0.05 to 0.25 mm, preferably 0.25 mm or 0.20 or 0.17 or 0.12 or 0.08.
It permits to obtain particles with an average particle size in the range from 40 to 80~.m.
as This capillary nozzle is schematically represented in Figure 2.
The spraying (nebulizing) nozzle, instead, is a two-component nozzle, which diameter is comprised between 0.05 and 0.25, preferably 0.25, and bearing both the mixture of the liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide and the simple gaseous carbon dioxide, acting as further atomizing agent. It permits to obtain particles with an average particle size in the range from 5 to 15 ~,m.
This spraying (nebulizing) nozzle is schematically represented in Figure 3.
It is envisaged that the gaseous carbon dioxide in the spraying (nebulizing) nozzle has a pressure from 1 to 10 bar and a temperature from 273 to 304 K, preferably a s pressure from 3.5 to 7.5 bar and a temperature from 291 to 301 K.
According to the invention, the source of liquid carbon dioxide is thermostated.
Preferably this condition is achieved by means of a thermostated cabinet wherein the source is disposed.
The process according to the invention or the apparatus according to the invention can to advantageously be used for homogenizing, pulverizing, pelletting, granulating and crystallizing is preferred.
For example, the process and the apparatus of the invention can advantageously be used to prepare microparticles useful in the food industry as well as in the cosmetic or chemical industry.
is The process of the invention and the apparatus of the invention are particularly suitable for producing lipid microparticles (microspheres) for pharmaceutical purposes. These microparticles may be constituted by polymers, lipids or mixtures thereof. The lipid or polymeric matrices can contain the active ingredient when they are sprayed in the process of the present invention or the active ingredient may be zo absorbed on their surface once the microparticles are produced through the process of the present invention.
In case of lipids several lipids with different hydrophilic/hydrophobic characteristics and chemical compositions can be used, such as for example tri-, di-and mono-glycerides, PEG- or PPG-glycerides, saccharide-glycerides, fatty acids, zs phospholipids and mixture thereof. Such lipid matrices may also contain pharmaceutically acceptable excipients, such as polymers having bioadhesive or absorption enhancing properties and selected from the group comprising or consisting of acrylic polymers (Carbopol~, Polycarbophil, Noveon~), medium chain fatty acids and polyethylene glycols, solubilizers (Cremophor~, Solutol~) The microparticle matrices can also be composed of hydrophilic or hydrophobic polymers, such as PEGS, Poloxamers (such as Lutrol~ F68, Lutrol~ F
127), polylactic acid (PLA), polyglycolic (PGA) acid, or poly(lactic-co-glycolic acid) (PLGA), polyvinylpyrrolidone (PVP), poly E caprolactone.
s The active ingredient may be a "small organic molecule" of any type or therapeutically effective peptide or protein. Therapeutically effective peptide or protein that may be incorporated into the lipid microparticles may be grouped into 3 main classes:
- regulatory factors including hormones, cytokines, lymphokines, io chemokines, their receptors and other regulatory factors of cellular growth and metabolism comprising enzymes;
- blood products including serum-derived blood factors and enzymatic fibrinogen activators;
- monoclonal antibodies.
is Proteins or peptides as above-mentioned include, but are not limited to, the following examples: AAT, UI~, PUK, streptokinase, tPA, SOD, insulin, GH, GRF, ANF, GnRH, LHRH analogs, erythropoietin, granulocyte CSF, granulocyte macrophage CSF, Interleukin-1, Interleukin-2, Interleukin-3lmultipotential CSF, Interleulcin-4, Interleul~in-5 (or Eosinophil-CSF), Interleulcin-6, Interleul~in-7, ao Interleukirl-8, Interleukin-9, Interleukin-10, Interleukin-11, interferon-a, interferon-(3, interferon-y, Leukemia inhibitory factor Macrophage CSF,TNF, Stem cell factor, RANTES and its variants, MCP-1 and its variants as well as receptors thereof.
According to a preferred embodiment of the invention, said protein or peptide is selected from the group consisting of Interleulcin-6, Interferon-oc, Interferon-(3, Zs Interferon-y, IL-18 Binding Protein, GnRH, LHRH analogs, GH, GRF, gonadotropins (like FSH, LH and hCG) and TNF receptors or soluble fragments thereof.
The process of the invention and the apparatus of the invention are also suitable for the micronization of small organic molecules, preferably but not exclusively poorly soluble, alone or in combination with known excipients, surfactants, self emulsifying s o agents The process and the apparatus according to the invention will now be described in more detail by way of examples with reference to Figures.
Description of the Figures Fi ure 1: Schematic representation of process and apparatus s Figure 2: Schematic representation of the capillary nozzle Fi ure 3: Schematic representation of the spraying (nebulizing) nozzle Fi ure 4: LM made of Imwitor 900 prepared with capillary nozzle Laser Diffractometer (LD) results of the Imwitor 900 LM batches prepared under io similar process conditions for reproducibility evaluation. (a) Trials with 0.25 mm product nozzle, (b) trials with 0.12 mm product nozzle. The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
is Figure 5: LD results of the Imwitor 900 LM batches prepared with the spraying (nebulizing) nozzle under similar process conditions for reproducibility evaluation.
The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma zo shaped) curves are average curves of three samples from the same batch.
Figure 6: LD results of the Compritol a ATO LM batches prepared using two different capillary flow nozzle diameters. The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch.
Frequency zs (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
Fi ure 7: LD results of the Compritol E ATO LM batches prepared with the spraying (nebulizing) nozzle under similar process conditions for reproducibility evaluation.
3o The Y error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
Fi ure 8: LD data and graphs (frequency (bell-shaped) and undersize (sigma-shaped) s curves) of the Compritol a ATO/PEG 6000 LM.
Examples Example 1 - Preparation of microparticles accordin, t~ o the process of the invention 1.1 Melting of the materials afzd drug incorporation into the mat~~ix:
The substances to be processed (lipid and/or polymer mixture) are melted in a io thermostated bath, at a proper temperature, depending on the substances used. A drug can be added to the molten matrix, under constant stirring. The molten mass is then poured into the feeding vessel of the atomizer, thermostated at a suitable temperature (so to keep the mass in the liquid form). Alternatively, this first melting step can be also performed directly in the feeding vessel of the atomizer, since such vessel is is equipped with a stirring tool.
Alternatively a certain amount of solvent can be added to the mixture. This would allow the incorporation of a drug into the matrix prior dissolution into a suitable solvent, or allow the preparation of compositions by intimately mixing different excipients (such as polymers and lipids of different types) 1.2 Material pr~ocessi~Zg The molten mass is then conveyed, under controlled pressure, through the nozzle (which is also therlnostated at a suitable temperature), to the spraying (nebulizing) tower, where microparticles form as a result of spraying (nebulizing) and cooling zs effect of liquid COZ. The product in powder form is then collected from an appropriate opening at the bottom of the spraying (nebulizing) tower.
1.3 Physico-chemical char~acterizatioh of the naicr~opar~ticles The microparticles described in the examples below have been characterized mainly 3o for their particle size. Thermal analysis and optical microscope analysis have also been performed on some samples.
1.3. Pat~ticle size analysis The microparticles/microspheres) were characterized for their particle size distribution using Laser Diffractometer (LD) Mastersizer Microplus MAF 5001 (Malvern). The small volume sample dispersion unit (100 ml capacity) was used for s the analysis. A slurry was first prepared adding about 50 ~.l of Tween 20 TM
( also known generically as Polysorbate 20; it is a surfactant; sorbitan mono-9octadecenoate poly(oxy 1,1-ethanedlyl)), as suspending agent, to 30-40 mg of microparticles (this amount of material gives an obscuration value between 10 and 30%, as requested by analysis criteria). 5 ml of deionized water were added stepwise to the slurry and the io obtained suspension was sonicated for 3 minutes. The suspension was then poured into the small volume unit and lcept circulating in the dispersion unit at a pump speed of 1500 rpm. Three measurements were taken for each sample and the data were processed using Fraunhofer presentation. Each batch was analyzed in triplicate.
The size of the population is described by the following size parameters:
is D (v, 0.1) means that 10% (in volume) of the particles have a diameter below this value.
D (v, 0.5) means that 50% (in volume) of the particles have a diameter below this value.
D (v, 0.9) means that 90% (in volume) of the particles have a diameter below this zo value.
Span is calculated as (D (v, 0.9 - D (v, 0.1)) / D (v, 0.5), and is a measure of the diameter distribution width.
1.3.2 Therynal D~e~~ential Scan~ai~cgAnalysis (DSC) araalysis zs The DSC analyses were performed in both heating and cooling mode, using the Pyris 1 Differential Scanning Calorimeter (Perlcin Elmer), at the following operative conditions:
Sample weight: 3-6 mg Range: 0°C-100 °C
3o Scan rate: 5 °C/min Pan capacity: SOpL (pan with holes) Purge gas (Nz) flow: 20 cc/min.
1.3.3 Morphology evaluation by optical microscope Optical microscope analyses were performed using the Axiolab A (Zeiss) optical microscope (Axiovision software).
s LM samples were placed on the microscope glass either as they are, or after suspension in water+Tween 20. For some samples, the suspension was analyzed after drying (at room conditions). The analysis was performed using SOx or 200x enlargement, under transmitted light, or, in few cases, in reflected light mode.
io Example 2 - Lipid Microparticles (LM) Materials In the examples described below the following materials were tested:
Imwitor 900 (glyceryl monostearate), Condea Compritol E ATO (glyceryl behenate), Gattefosse is Lutrol E 6000 (PEG 6000), Basf Gelucire 50/13 (Stearoyl Macrogol glyceride: mixture of mono-, di- and triglycerides and mono- and di-fatty acid esters of polyethylene glycol), Gattefosse 2.1 Preparation of LM with the capillary flow nozzle using two d~er~ent nozzle ao sizes 200 g of Imwitor 900 were melted in a thermostated water bath (75°C), poured into the feeding vessel and processed at the following process conditions:
Product nozzle 0.12 and ~ 0.25 mm L COz nozzle 0.25 mm ~
Product nozzle 115C
temperature Oven temperature90C
Gaseous COZ pressure2 bar in the feeding vessel L COz pressure about 60 bar Replicates were performed, and the results of the particle size analysis are shown in Fig. 4. The particle size was also verified by optical microscope.
2.2 Preparation of Inzwitor 900 LM using the spraying (nebulizin~ nozzle s 200 g of Imwitor 900 were melted in a thermostated water bath (75°C), poured into the feeding vessel and processed at the following process conditions:
L C02 nozzle 0.25 mm Product nozzle 115C
temperature io Oven temperature90C
Gaseous C02 pressure2-3 bar in the feeding vessel Gaseous C02 pressure5 bar in the product nozzle is L C02 pressure about 60 ~ bar Replicates were performed, and the results of the particle size analysis are shown in Fig. 5. The particle size was also verified by optical microscope.
20 2.3 Py°eparation of LM made of Coynpritol E ATO With the capillary flow nozzle using two d~ej°e~zt nozzle sizes 200 g of Compritol E ATO were melted in a thermostated water bath (85°C), poured into the feeding vessel and processed at the following process conditions:
Product nozzle 0.12 and Q~ 0.20 mlll L C02 nozzle ~ 0.25 mm Product nozzle 115C
temperature Oven temperature 110C
Gaseous C02 pressure2 bar in the feeding vessel L C02 pressure about 55 bar The results of the particle size analysis are shown in Fig. 6. The particle size was also verified by optical microscope.
s 2.4 Preparation of Compritol E ATO LM using tire spraying (nebulizing) nozzle 200 g of Compritol E ATO were melted in a thennostated water bath (85°C), poured into the feeding vessel and processed at the following process conditions:
L COz nozzle Q~ 0.25 mm Product nozzle 115C
io temperature Oven temperature 90C
Gaseous COz pressure3 bar in the feeding vessel Gaseous COz pressure5 bar in is the product nozzle L COz pressure about 60 bar Two replicates were performed, and the results of the particle size analysis are shown in Fig. 7. The particle size was also verified by optical microscope.
zo 2.5 Preparation of Coynpritol E ATO - PEG 6000 LM using the capillary flow nozzle 200 g of a Compritol E ATO/PEG 6000 (8:2) mixture were melted in a thermostated water bath (85°C), poured into the feeding vessel and processed at the following zs process conditions:
Product nozzle 0.25 mm Q~
L COz nozzle ~ 0.25 mm Product nozzle 130C
s temperature Oven temperature 100C
Gaseous COz pressure2 bar in the feeding vessel L COz pressure about 55 bar io The results of the particle size analysis are shown in Fig. 8. The particle size was also verified by optical microscope.
2. 6 Prepaf°atio~r of Gelucire 50/13 LMusiug the capillafy flow nozzle 200 g of Gelucire 50/13 were melted in a thermostated water bath (60°C), poured into is the feeding vessel and processed at the following process conditions:
Product nozzle 0.25 mm ~3 L COz nozzle 0.25 mm QS
Product nozzle 60C
temperature o Oven temperature60C
Gaseous COz pressureabout 4 bar in the feeding vessel L COz pressure about 60 bar zs LD analysis was not performed, due to material partial solubilization in water (normally used as medium for LD analysis). The particle size of the product was also evaluated by optical microscope analysis.
2.7 P~epar~atiofz of Gelucif°e 50/13 LMusifzg tlae sprayifzg (nebulizin~ nozzle 30 100 g of Gelucire 50/13 were melted in a therinostated water bath (60°C), poured into the feeding vessel and processed at the following process conditions:
L COZ nozzle ~ 0.25 mm Product nozzle 100C
temperature Oven temperature 80C
Gaseous COZ pressure2 bar in the feeding vessel Gaseous COZ pressure2.5 bar in the product nozzle L COZ pressure about 60 bar io LD analysis was not performed, due to material partial solubilization in water (normally used as medium for LD analysis). The particle size of the product was also evaluated by optical microscope analysis.
Conclusions is As shown in the Examples reported above, the process of the present invention allows to prepare microparticles having the following advantageous characteristics:
~ controlled particle size of the product: D (v, 0.5) around 40-80 pm when using capillaf~y flow nozzle, and down to 15 ~,m, or 10 pm (possibly 5 ~.m) when using the sprayi~rg (yzebulizing) nozzle (these data refer to the material tested 2o so far, that is mainly Imwitor 900 and Compritol E ATO) ~ Relatively narrow size distribution ~ Spherical shape of the particles Such characteristics lead to applications as injectable microparticles, but also as 2s delivery systems for oral, nasal and, potentially, pulmonary administration route.
mixture of substances and gaseous carbon pass, under pressure, through a nozzle and expand in a spray tower. Simultaneously, from a fiu~ther nozzle, liquid carbon dioxide is sprayed in the spray tower. The contact between sprayed liquid or pasty substances/
mixture of s substances and liquid carbon dioxide causes the instantaneous cooling and atomization of the liquid or pasty substances/ mixture of substances. A
schematic representation of the process and apparatus is reported in Figure 1.
During the expansion, small particles of liquid or pasty substances/ mixture of substances, spherically-shaped are formed. This leads to a good reproducibility of the io process and to a fme particulate with an average diameter comprises between 2 and 100 ~.m, preferably in ranges of from 5 to 15 ~.m or from 40 to 80 ~.m, depending on the nozzle used. Moreover, the particles are always spherically shaped and have a narrow particle size distribution.
Therefore the main object of the invention is to provide a process for cooling and is atomizing liquid or pasty substance or mixture of substances, in which a liquid or pasty substance / mixture of substances is combined with gaseous carbon dioxide and the mixture of liquid or pasty substance / mixture of substances and gaseous carbon dioxide is then expanded and cooled by contacting a flux of liquid carbon dioxide, as a result the substance / mixture of substances is cooled and atomized.
zo A further advantage according to the invention is that by varying the flow ratios of substances/ mixture of substances from the first nozzle and the liquid carbon dioxide from the other nozzle, the final temperature obtained may be varied within broad ranges.
It is envisaged that the liquid carbon dioxide has a pressure from 6 to 72 bar and a zs temperature from 216 to 304 K, preferably a pressure from 30 to 70 bar and a temperature from 230 to 304 K, and particularly a pressure from 50 to 68 bar and a temperature from 291 to 301 K.
The pressure of gaseous carbon dioxide in the storage vessel is comprised between 1 to 10 bar, preferably in a range from 1.2 and 4.5 bar. The temperature of the gaseous carbon dioxide in the storage vessel is normally comprised between 273 and 304 K, preferably between 291 and 301 K.
This procedure has the advantage that at a preferred pressure range and temperature range the carbon dioxide can be taken off directly from the supply system, for s example low-pressure and medium-pressure tanks or carbon dioxide cylinders, without further gas treatment.
According to the invention the mixture of liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide and the liquid carbon dioxide are expanded at pressure from 0 to 60 bar, preferably to a pressure from 0 to 20 bar, and particularly to preferably to approximately 1 bar. The expansion to atmospheric pressure (approximately 1 bar) has the advantage that filling can be performed directly into an non-pressurized system.
According to the invention the liquid or pasty substance/ mixture of substances and/or the gaseous carbon dioxide and/or the mixture of liquid or pasty substance/
mixture of is substances and the gaseous carbon dioxide can be fed to al least one heatable or coolable line. Using a heatable or coolable line, the temperature for the liquid or pasty substance/ mixture of substances and/or the gaseous carbon dioxide and/or the mixture of liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide can be controlled, in order to set the desired or required process temperature.
zo According to the invention the liquid or pasty substance/ mixture of substances is mixed with the gaseous carbon dioxide in the storage vessel, thanks to a stirrer disposed in such vessel.
The object is further achieved by an apparatus for cooling liquid or pasty substance or mixture of substances which comprises:
zs a. a storage vessel for the liquid or pasty substance/ mixture of substances, to which is allocated a line, in which a device for transporting the liquid or pasty substance/ mixture of substances is disposed, b. a source of liquid carbon dioxide, to which source is allocated a line, c. a source of gaseous carbon dioxide, to which source is allocated a line which line has a connection with the line transporting the liquid or pasty substance/ mixture of substances, s d. an expansion chamber in which the liquid carbon dioxide and the liquid or pasty substance/ mixture of substances mixed with the gaseous carbon dioxide are conveyed.
The apparatus is constructed in such a manner that the mixture of liquid or pasty substance/ mixture of substances and gaseous carbon dioxide is not expanded until on io exit from the expansion apparatus. A very direct contact takes place out between liquid or pasty substance/ mixture of substances and liquid carbon dioxide achieving cooling and atomization of liquid or pasty substance/ mixture of substances in the spray tower. The apparatus ensures rapid cooling and atomization of the liquid or pasty substance/ mixture of substances. By use of the inventive expansion apparatus, is small, easily flowable particles of the liquid or pasty substance/ mixture of substances are produced.
Advantageously, the lines or apparatuses or devices bearing the liquid or pasty substance/ mixture of substances and/or gaseous carbon dioxide and/or liquid carbon dioxide and/or the lines or apparatuses or devices bearing the mixture of the liquid or ao pasty substance/ mixture of substances and gaseous carbon dioxide have apparatuses for their heating or cooling, in order to set the desired or required temperature in the individual trains bearing carbon dioxide and/or substance/ mixture of substances. The lines) should preferably be heated or cooled separately. Piping having internals for heating is preferred.
zs It is envisaged that an apparatus for heating or cooling is allocated to the line allocated to the storage vessel for the liquid or pasty substance/ mixture of substances.
According to the invention, the expansion apparatus has two valves and two nozzles.
The valves used can be open/closed valve or control valves and they are disposed in the lines connecting the spray tower to the storage vessel and the source of liquid carbon dioxide.
The nozzles for the liquid carbon dioxide and for the mixture of liquid or pasty s substance/ mixture of substances and gaseous carbon dioxide, advantageously, have a shielding device, preferably a jacket tube. The use of a nozzle having a jacket tube has the advantage that only a small amount of air is taken in or sucked into the stream.
The carbon dioxide in this case is at least partially converted into carbon dioxide snow. Typically, approximately 30% by weight of carbon dioxide snow and io approximately 70% by weight of gaseous carbon dioxide are formed during the expansion of the liquid carbon dioxide at the nozzle.
Preferably, the tubes of these expansion devices are prepared. This can be performed by polishing or coating or separate heating. According to the invention a coating with Teflon of the inside of the tubes of the expansion devices are particularly preferred.
is Furthermore, according to the invention, the nozzle for the expansion of the mixture of the liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide, advantageously, has, at its bottom, an isolating coating in order to prevent the obstruction due to the cooled substance on its surface.
According to the invention the nozzle for the expansion of the mixture of the liquid or zo pasty substance/ mixture of substances and the gaseous carbon dioxide can be a capillary flow nozzle or a spraying (nebulizing) nozzle.
The capillary flow nozzle is a one-component nozzle, which diameter is comprised between 0.05 to 0.25 mm, preferably 0.25 mm or 0.20 or 0.17 or 0.12 or 0.08.
It permits to obtain particles with an average particle size in the range from 40 to 80~.m.
as This capillary nozzle is schematically represented in Figure 2.
The spraying (nebulizing) nozzle, instead, is a two-component nozzle, which diameter is comprised between 0.05 and 0.25, preferably 0.25, and bearing both the mixture of the liquid or pasty substance/ mixture of substances and the gaseous carbon dioxide and the simple gaseous carbon dioxide, acting as further atomizing agent. It permits to obtain particles with an average particle size in the range from 5 to 15 ~,m.
This spraying (nebulizing) nozzle is schematically represented in Figure 3.
It is envisaged that the gaseous carbon dioxide in the spraying (nebulizing) nozzle has a pressure from 1 to 10 bar and a temperature from 273 to 304 K, preferably a s pressure from 3.5 to 7.5 bar and a temperature from 291 to 301 K.
According to the invention, the source of liquid carbon dioxide is thermostated.
Preferably this condition is achieved by means of a thermostated cabinet wherein the source is disposed.
The process according to the invention or the apparatus according to the invention can to advantageously be used for homogenizing, pulverizing, pelletting, granulating and crystallizing is preferred.
For example, the process and the apparatus of the invention can advantageously be used to prepare microparticles useful in the food industry as well as in the cosmetic or chemical industry.
is The process of the invention and the apparatus of the invention are particularly suitable for producing lipid microparticles (microspheres) for pharmaceutical purposes. These microparticles may be constituted by polymers, lipids or mixtures thereof. The lipid or polymeric matrices can contain the active ingredient when they are sprayed in the process of the present invention or the active ingredient may be zo absorbed on their surface once the microparticles are produced through the process of the present invention.
In case of lipids several lipids with different hydrophilic/hydrophobic characteristics and chemical compositions can be used, such as for example tri-, di-and mono-glycerides, PEG- or PPG-glycerides, saccharide-glycerides, fatty acids, zs phospholipids and mixture thereof. Such lipid matrices may also contain pharmaceutically acceptable excipients, such as polymers having bioadhesive or absorption enhancing properties and selected from the group comprising or consisting of acrylic polymers (Carbopol~, Polycarbophil, Noveon~), medium chain fatty acids and polyethylene glycols, solubilizers (Cremophor~, Solutol~) The microparticle matrices can also be composed of hydrophilic or hydrophobic polymers, such as PEGS, Poloxamers (such as Lutrol~ F68, Lutrol~ F
127), polylactic acid (PLA), polyglycolic (PGA) acid, or poly(lactic-co-glycolic acid) (PLGA), polyvinylpyrrolidone (PVP), poly E caprolactone.
s The active ingredient may be a "small organic molecule" of any type or therapeutically effective peptide or protein. Therapeutically effective peptide or protein that may be incorporated into the lipid microparticles may be grouped into 3 main classes:
- regulatory factors including hormones, cytokines, lymphokines, io chemokines, their receptors and other regulatory factors of cellular growth and metabolism comprising enzymes;
- blood products including serum-derived blood factors and enzymatic fibrinogen activators;
- monoclonal antibodies.
is Proteins or peptides as above-mentioned include, but are not limited to, the following examples: AAT, UI~, PUK, streptokinase, tPA, SOD, insulin, GH, GRF, ANF, GnRH, LHRH analogs, erythropoietin, granulocyte CSF, granulocyte macrophage CSF, Interleukin-1, Interleukin-2, Interleukin-3lmultipotential CSF, Interleulcin-4, Interleul~in-5 (or Eosinophil-CSF), Interleulcin-6, Interleul~in-7, ao Interleukirl-8, Interleukin-9, Interleukin-10, Interleukin-11, interferon-a, interferon-(3, interferon-y, Leukemia inhibitory factor Macrophage CSF,TNF, Stem cell factor, RANTES and its variants, MCP-1 and its variants as well as receptors thereof.
According to a preferred embodiment of the invention, said protein or peptide is selected from the group consisting of Interleulcin-6, Interferon-oc, Interferon-(3, Zs Interferon-y, IL-18 Binding Protein, GnRH, LHRH analogs, GH, GRF, gonadotropins (like FSH, LH and hCG) and TNF receptors or soluble fragments thereof.
The process of the invention and the apparatus of the invention are also suitable for the micronization of small organic molecules, preferably but not exclusively poorly soluble, alone or in combination with known excipients, surfactants, self emulsifying s o agents The process and the apparatus according to the invention will now be described in more detail by way of examples with reference to Figures.
Description of the Figures Fi ure 1: Schematic representation of process and apparatus s Figure 2: Schematic representation of the capillary nozzle Fi ure 3: Schematic representation of the spraying (nebulizing) nozzle Fi ure 4: LM made of Imwitor 900 prepared with capillary nozzle Laser Diffractometer (LD) results of the Imwitor 900 LM batches prepared under io similar process conditions for reproducibility evaluation. (a) Trials with 0.25 mm product nozzle, (b) trials with 0.12 mm product nozzle. The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
is Figure 5: LD results of the Imwitor 900 LM batches prepared with the spraying (nebulizing) nozzle under similar process conditions for reproducibility evaluation.
The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma zo shaped) curves are average curves of three samples from the same batch.
Figure 6: LD results of the Compritol a ATO LM batches prepared using two different capillary flow nozzle diameters. The error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch.
Frequency zs (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
Fi ure 7: LD results of the Compritol E ATO LM batches prepared with the spraying (nebulizing) nozzle under similar process conditions for reproducibility evaluation.
3o The Y error bars in the histogram graph refer to the standard deviation calculated on three samples from the same batch. Frequency (bell shaped) and undersize (sigma shaped) curves are average curves of three samples from the same batch.
Fi ure 8: LD data and graphs (frequency (bell-shaped) and undersize (sigma-shaped) s curves) of the Compritol a ATO/PEG 6000 LM.
Examples Example 1 - Preparation of microparticles accordin, t~ o the process of the invention 1.1 Melting of the materials afzd drug incorporation into the mat~~ix:
The substances to be processed (lipid and/or polymer mixture) are melted in a io thermostated bath, at a proper temperature, depending on the substances used. A drug can be added to the molten matrix, under constant stirring. The molten mass is then poured into the feeding vessel of the atomizer, thermostated at a suitable temperature (so to keep the mass in the liquid form). Alternatively, this first melting step can be also performed directly in the feeding vessel of the atomizer, since such vessel is is equipped with a stirring tool.
Alternatively a certain amount of solvent can be added to the mixture. This would allow the incorporation of a drug into the matrix prior dissolution into a suitable solvent, or allow the preparation of compositions by intimately mixing different excipients (such as polymers and lipids of different types) 1.2 Material pr~ocessi~Zg The molten mass is then conveyed, under controlled pressure, through the nozzle (which is also therlnostated at a suitable temperature), to the spraying (nebulizing) tower, where microparticles form as a result of spraying (nebulizing) and cooling zs effect of liquid COZ. The product in powder form is then collected from an appropriate opening at the bottom of the spraying (nebulizing) tower.
1.3 Physico-chemical char~acterizatioh of the naicr~opar~ticles The microparticles described in the examples below have been characterized mainly 3o for their particle size. Thermal analysis and optical microscope analysis have also been performed on some samples.
1.3. Pat~ticle size analysis The microparticles/microspheres) were characterized for their particle size distribution using Laser Diffractometer (LD) Mastersizer Microplus MAF 5001 (Malvern). The small volume sample dispersion unit (100 ml capacity) was used for s the analysis. A slurry was first prepared adding about 50 ~.l of Tween 20 TM
( also known generically as Polysorbate 20; it is a surfactant; sorbitan mono-9octadecenoate poly(oxy 1,1-ethanedlyl)), as suspending agent, to 30-40 mg of microparticles (this amount of material gives an obscuration value between 10 and 30%, as requested by analysis criteria). 5 ml of deionized water were added stepwise to the slurry and the io obtained suspension was sonicated for 3 minutes. The suspension was then poured into the small volume unit and lcept circulating in the dispersion unit at a pump speed of 1500 rpm. Three measurements were taken for each sample and the data were processed using Fraunhofer presentation. Each batch was analyzed in triplicate.
The size of the population is described by the following size parameters:
is D (v, 0.1) means that 10% (in volume) of the particles have a diameter below this value.
D (v, 0.5) means that 50% (in volume) of the particles have a diameter below this value.
D (v, 0.9) means that 90% (in volume) of the particles have a diameter below this zo value.
Span is calculated as (D (v, 0.9 - D (v, 0.1)) / D (v, 0.5), and is a measure of the diameter distribution width.
1.3.2 Therynal D~e~~ential Scan~ai~cgAnalysis (DSC) araalysis zs The DSC analyses were performed in both heating and cooling mode, using the Pyris 1 Differential Scanning Calorimeter (Perlcin Elmer), at the following operative conditions:
Sample weight: 3-6 mg Range: 0°C-100 °C
3o Scan rate: 5 °C/min Pan capacity: SOpL (pan with holes) Purge gas (Nz) flow: 20 cc/min.
1.3.3 Morphology evaluation by optical microscope Optical microscope analyses were performed using the Axiolab A (Zeiss) optical microscope (Axiovision software).
s LM samples were placed on the microscope glass either as they are, or after suspension in water+Tween 20. For some samples, the suspension was analyzed after drying (at room conditions). The analysis was performed using SOx or 200x enlargement, under transmitted light, or, in few cases, in reflected light mode.
io Example 2 - Lipid Microparticles (LM) Materials In the examples described below the following materials were tested:
Imwitor 900 (glyceryl monostearate), Condea Compritol E ATO (glyceryl behenate), Gattefosse is Lutrol E 6000 (PEG 6000), Basf Gelucire 50/13 (Stearoyl Macrogol glyceride: mixture of mono-, di- and triglycerides and mono- and di-fatty acid esters of polyethylene glycol), Gattefosse 2.1 Preparation of LM with the capillary flow nozzle using two d~er~ent nozzle ao sizes 200 g of Imwitor 900 were melted in a thermostated water bath (75°C), poured into the feeding vessel and processed at the following process conditions:
Product nozzle 0.12 and ~ 0.25 mm L COz nozzle 0.25 mm ~
Product nozzle 115C
temperature Oven temperature90C
Gaseous COZ pressure2 bar in the feeding vessel L COz pressure about 60 bar Replicates were performed, and the results of the particle size analysis are shown in Fig. 4. The particle size was also verified by optical microscope.
2.2 Preparation of Inzwitor 900 LM using the spraying (nebulizin~ nozzle s 200 g of Imwitor 900 were melted in a thermostated water bath (75°C), poured into the feeding vessel and processed at the following process conditions:
L C02 nozzle 0.25 mm Product nozzle 115C
temperature io Oven temperature90C
Gaseous C02 pressure2-3 bar in the feeding vessel Gaseous C02 pressure5 bar in the product nozzle is L C02 pressure about 60 ~ bar Replicates were performed, and the results of the particle size analysis are shown in Fig. 5. The particle size was also verified by optical microscope.
20 2.3 Py°eparation of LM made of Coynpritol E ATO With the capillary flow nozzle using two d~ej°e~zt nozzle sizes 200 g of Compritol E ATO were melted in a thermostated water bath (85°C), poured into the feeding vessel and processed at the following process conditions:
Product nozzle 0.12 and Q~ 0.20 mlll L C02 nozzle ~ 0.25 mm Product nozzle 115C
temperature Oven temperature 110C
Gaseous C02 pressure2 bar in the feeding vessel L C02 pressure about 55 bar The results of the particle size analysis are shown in Fig. 6. The particle size was also verified by optical microscope.
s 2.4 Preparation of Compritol E ATO LM using tire spraying (nebulizing) nozzle 200 g of Compritol E ATO were melted in a thennostated water bath (85°C), poured into the feeding vessel and processed at the following process conditions:
L COz nozzle Q~ 0.25 mm Product nozzle 115C
io temperature Oven temperature 90C
Gaseous COz pressure3 bar in the feeding vessel Gaseous COz pressure5 bar in is the product nozzle L COz pressure about 60 bar Two replicates were performed, and the results of the particle size analysis are shown in Fig. 7. The particle size was also verified by optical microscope.
zo 2.5 Preparation of Coynpritol E ATO - PEG 6000 LM using the capillary flow nozzle 200 g of a Compritol E ATO/PEG 6000 (8:2) mixture were melted in a thermostated water bath (85°C), poured into the feeding vessel and processed at the following zs process conditions:
Product nozzle 0.25 mm Q~
L COz nozzle ~ 0.25 mm Product nozzle 130C
s temperature Oven temperature 100C
Gaseous COz pressure2 bar in the feeding vessel L COz pressure about 55 bar io The results of the particle size analysis are shown in Fig. 8. The particle size was also verified by optical microscope.
2. 6 Prepaf°atio~r of Gelucire 50/13 LMusiug the capillafy flow nozzle 200 g of Gelucire 50/13 were melted in a thermostated water bath (60°C), poured into is the feeding vessel and processed at the following process conditions:
Product nozzle 0.25 mm ~3 L COz nozzle 0.25 mm QS
Product nozzle 60C
temperature o Oven temperature60C
Gaseous COz pressureabout 4 bar in the feeding vessel L COz pressure about 60 bar zs LD analysis was not performed, due to material partial solubilization in water (normally used as medium for LD analysis). The particle size of the product was also evaluated by optical microscope analysis.
2.7 P~epar~atiofz of Gelucif°e 50/13 LMusifzg tlae sprayifzg (nebulizin~ nozzle 30 100 g of Gelucire 50/13 were melted in a therinostated water bath (60°C), poured into the feeding vessel and processed at the following process conditions:
L COZ nozzle ~ 0.25 mm Product nozzle 100C
temperature Oven temperature 80C
Gaseous COZ pressure2 bar in the feeding vessel Gaseous COZ pressure2.5 bar in the product nozzle L COZ pressure about 60 bar io LD analysis was not performed, due to material partial solubilization in water (normally used as medium for LD analysis). The particle size of the product was also evaluated by optical microscope analysis.
Conclusions is As shown in the Examples reported above, the process of the present invention allows to prepare microparticles having the following advantageous characteristics:
~ controlled particle size of the product: D (v, 0.5) around 40-80 pm when using capillaf~y flow nozzle, and down to 15 ~,m, or 10 pm (possibly 5 ~.m) when using the sprayi~rg (yzebulizing) nozzle (these data refer to the material tested 2o so far, that is mainly Imwitor 900 and Compritol E ATO) ~ Relatively narrow size distribution ~ Spherical shape of the particles Such characteristics lead to applications as injectable microparticles, but also as 2s delivery systems for oral, nasal and, potentially, pulmonary administration route.
Claims (22)
1. A process for cooling and atomizing liquid or pasty substance or mixture of substances, in which a liquid or pasty substance / mixture of substances is combined with gaseous carbon dioxide and the mixture of liquid or pasty substance / mixture of substances and gaseous carbon dioxide is then expanded and cooled by contacting a flux of liquid carbon dioxide, as a result the substance / mixture of substances is cooled and atomized.
2. The process according to claim 1, in which the liquid carbon dioxide has a pressure of from 6 to 72 bar and a temperature of 216 to 304 K.
3. The process according to claim 1, in which the liquid carbon dioxide has a pressure of from 30 to 70 bar and a temperature of from 230 to 304 K.
4. The process according to claim 1, in which the gaseous carbon dioxide has a pressure of from 50 to 68 bar and a temperature of from 291 to 301 K.
5. The process according to claim 3, in which the gaseous carbon dioxide in the storage vessel has a pressure of from 1 to 10 bar and a temperature of from 273 to 304 K.
6. The process according to any one of claims 1 to 5, in which the liquid or pasty substance/ mixture of substances and/or the mixture of liquid or pasty substance/ mixture of substances and gaseous carbon dioxide is or are fed to at least one heatable or coolable line.
7. The process according to claim 1, in which the final average particle size is comprised in a range between 2 and 100 µm.
8. The process according to claim 7, in which the final average particle size is comprised in a range between 40 to 80 µm.
9. The process according to claim 7, in which the final average particle size is comprised in a range between 5 and 15 µm.
10. The process according to any one of claims 1 to 9, in which the liquid or pasty substance/ mixture of substances is mixed with the gaseous carbon dioxide in the storage vessel by means of a stirrer disposed in such vessel.
11. An apparatus for cooling liquid or pasty substance or mixture of substances which comprises:
(a) a storage vessel for the liquid or pasty substance/ mixture of substances, to which is allocated a line, in which a device for transporting the liquid or pasty substance/ mixture of substances is disposed, (b) a source of liquid carbon dioxide, to which source is allocated a line, (c) a source of gaseous carbon dioxide, to which source is allocated a line which line has a connection with the line transporting the liquid or pasty substance/ mixture of substances, (d) an expansion chamber in which the liquid carbon dioxide and the liquid or pasty substance/ mixture of substances mixed with the gaseous carbon dioxide are conveyed.
(a) a storage vessel for the liquid or pasty substance/ mixture of substances, to which is allocated a line, in which a device for transporting the liquid or pasty substance/ mixture of substances is disposed, (b) a source of liquid carbon dioxide, to which source is allocated a line, (c) a source of gaseous carbon dioxide, to which source is allocated a line which line has a connection with the line transporting the liquid or pasty substance/ mixture of substances, (d) an expansion chamber in which the liquid carbon dioxide and the liquid or pasty substance/ mixture of substances mixed with the gaseous carbon dioxide are conveyed.
12. The apparatus according to claim 11, in which an apparatus for heating or cooling the line is disposed in the line allocated to the source of gaseous carbon dioxide.
13. The apparatus according to claim 11 or 12, wherein the source of gaseous and liquid carbon dioxide is contained in a thermostated cabinet.
14. The apparatus according to any one of claims 11 to 13, in which an apparatus for heating or cooling the line is allocated to the line allocated to the storage vessel for the liquid or pasty substance/ mixture of substances.
15. The apparatus according to any one of claims 11 to 14, in which an apparatus for mixing is allocated to the storage vessel for the liquid or pasty substance/
mixture of substances.
mixture of substances.
16. The apparatus according to any one of claims 11 to 15, in which the expansion chamber has two nozzles and two valves.
17. The apparatus according to claim 16, in which the two nozzles and the two valves have an isolating coating.
18. The apparatus according to claim 16 or 17, in which the two nozzles are a capillary flow nozzle or a spraying nozzle.
19. The apparatus according to claim 17 or 18, in which the two valves are an open/closed valve or a control valve.
20. The use of the process according to claim 1 or of the apparatus according to claim 11 for pulverizing, pelleting, granulating and crystallizing.
21. The use of the process according to claim 1 or of the apparatus according to claim 11 for the production of microparticles for pharmaceutical uses.
22. The use of the process according to claim 1 or of the apparatus according to claim 11, wherein the microparticles contain one or more therapeutic active substances.
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| EP03104024.9 | 2003-10-30 | ||
| EP03104024 | 2003-10-30 | ||
| PCT/EP2004/052674 WO2005049192A1 (en) | 2003-10-30 | 2004-10-27 | Process and apparatus for cooling and atomizing liquid or pasty-like substances |
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| CA2541404C true CA2541404C (en) | 2012-12-11 |
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| US (2) | US20070079629A1 (en) |
| EP (1) | EP1677903B1 (en) |
| JP (2) | JP5037944B2 (en) |
| AU (1) | AU2004291337B2 (en) |
| CA (1) | CA2541404C (en) |
| ES (1) | ES2392433T3 (en) |
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| CA2473345A1 (en) * | 2004-07-08 | 2006-01-08 | Adam Stern | Apparatus and method for the prevention of polar ice mass depletion |
| US7838522B2 (en) | 2004-11-17 | 2010-11-23 | Ares Trading S.A. | Benzothiazole formulations and use thereof |
| BRPI0613042A2 (en) | 2005-07-15 | 2010-12-14 | Serono Lab | jnk inhibitors for the treatment of endometriosis |
| KR20080044836A (en) | 2005-07-15 | 2008-05-21 | 라보라뚜와르 세로노 에스. 에이. | Jnk inhibitors for the treatment of endometriosis |
| EP2298286B8 (en) * | 2009-09-18 | 2017-08-09 | SiTec PharmaBio SL | Process for dewatering of product powders |
| DE102015007604A1 (en) | 2015-06-12 | 2016-12-29 | Messer France S.A.S | Apparatus and method for cooling and atomising liquid or pasty substances |
| CN106074672B (en) * | 2016-07-18 | 2021-10-29 | 四川科伦药业股份有限公司 | Constant temperature system for improving quality of fat milk product |
| US10234186B1 (en) * | 2017-11-09 | 2019-03-19 | James Chun Koh | Apparatus for manufacturing powdered ice with salinity |
| CN109717356B (en) * | 2019-03-08 | 2022-03-08 | 中国科学院西北高原生物研究所 | Fresh cordyceps sinensis quick-freezing preservation method combining liquid nitrogen with liquid carbon dioxide |
| FR3094649B1 (en) | 2019-04-05 | 2021-12-10 | Air Liquide | Spray drying powder production processes |
| EP4190437A1 (en) | 2021-12-03 | 2023-06-07 | SiTec PharmaBio SL | Process and apparatus for the manufacture of solid microparticles |
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| JPH06185B2 (en) * | 1985-04-20 | 1994-01-05 | ノードソン株式会社 | Spray-type granulation method of heat-fusible substance and its granulation apparatus |
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| DE3744329A1 (en) * | 1987-12-28 | 1989-07-06 | Schwarz Pharma Gmbh | METHOD FOR THE PRODUCTION OF AT LEAST ONE ACTIVE AGENT AND A TRAITER COMPRISING PREPARATION |
| CH677141A5 (en) * | 1988-09-16 | 1991-04-15 | Rosenmund Ag | |
| US4952224A (en) * | 1989-04-17 | 1990-08-28 | Canadian Oxygen Limited | Method and apparatus for cryogenic crystallization of fats |
| US5549922A (en) * | 1989-04-24 | 1996-08-27 | Juchem Gmbh | Method of making flour-containing edible semifinished products |
| US4952223A (en) * | 1989-08-21 | 1990-08-28 | The Boc Group, Inc. | Method and apparatus of producing carbon dioxide in high yields from low concentration carbon dioxide feeds |
| US5121611A (en) * | 1990-10-25 | 1992-06-16 | Liquid Carbonic Corporation | Refrigeration apparatus and method of refrigeration |
| US6086833A (en) * | 1997-09-08 | 2000-07-11 | Air Liquide America Corporation | Process and equipment for sanitizing and packaging food using ozone |
| JP3492317B2 (en) * | 1997-10-06 | 2004-02-03 | アーダルベルト−ラプス−シュティフツング | Process for producing powdery products from liquid substances or mixed substances |
| DE19748069A1 (en) * | 1997-10-31 | 1999-05-06 | Messer Griesheim Gmbh | Method and device for cooling and atomizing liquid or pasty substances |
| SE9901059L (en) * | 1999-03-22 | 2000-09-23 | Johan Carlfors | Method for making particles |
| JP3225032B2 (en) * | 1999-10-28 | 2001-11-05 | 味の素株式会社 | Temperature control method and temperature control device for kneading edible dough |
| JP2004517699A (en) * | 2001-01-30 | 2004-06-17 | ボード オブ リージェンツ ユニバーシティ オブ テキサス システム | Method for producing nanoparticles and microparticles by spray freezing into liquid |
| TW586963B (en) * | 2001-07-20 | 2004-05-11 | Nektar Therapeutics Uk Ltd | Method and apparatus for preparing target substance in particulate form and fluid inlet assembly for said apparatus |
| GB0117696D0 (en) * | 2001-07-20 | 2001-09-12 | Bradford Particle Design Plc | Particle information |
| US7582284B2 (en) * | 2002-04-17 | 2009-09-01 | Nektar Therapeutics | Particulate materials |
| US6931888B2 (en) * | 2003-02-07 | 2005-08-23 | Ferro Corporation | Lyophilization method and apparatus for producing particles |
-
2004
- 2004-10-27 EP EP04791318A patent/EP1677903B1/en not_active Revoked
- 2004-10-27 AU AU2004291337A patent/AU2004291337B2/en not_active Ceased
- 2004-10-27 WO PCT/EP2004/052674 patent/WO2005049192A1/en active Application Filing
- 2004-10-27 JP JP2006537294A patent/JP5037944B2/en not_active Expired - Fee Related
- 2004-10-27 ES ES04791318T patent/ES2392433T3/en active Active
- 2004-10-27 US US10/577,929 patent/US20070079629A1/en not_active Abandoned
- 2004-10-27 CA CA2541404A patent/CA2541404C/en not_active Expired - Fee Related
-
2006
- 2006-04-25 IL IL175171A patent/IL175171A/en not_active IP Right Cessation
- 2006-05-22 NO NO20062311A patent/NO20062311L/en not_active Application Discontinuation
-
2008
- 2008-08-21 US US12/195,625 patent/US20090211265A1/en not_active Abandoned
-
2012
- 2012-04-04 JP JP2012085640A patent/JP2012161796A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012161796A (en) | 2012-08-30 |
| WO2005049192A1 (en) | 2005-06-02 |
| NO20062311L (en) | 2006-05-22 |
| EP1677903A1 (en) | 2006-07-12 |
| EP1677903B1 (en) | 2012-08-01 |
| US20090211265A1 (en) | 2009-08-27 |
| AU2004291337A1 (en) | 2005-06-02 |
| ES2392433T3 (en) | 2012-12-10 |
| JP2007509739A (en) | 2007-04-19 |
| IL175171A (en) | 2010-12-30 |
| AU2004291337B2 (en) | 2009-12-03 |
| CA2541404A1 (en) | 2005-06-02 |
| US20070079629A1 (en) | 2007-04-12 |
| IL175171A0 (en) | 2006-09-05 |
| JP5037944B2 (en) | 2012-10-03 |
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